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EP0543363B1 - Dimères fluorés d'aldocetènes, et leur utilisation comme agents de collage hydrophobe et oléophobe pour matériaux cellulosiques - Google Patents

Dimères fluorés d'aldocetènes, et leur utilisation comme agents de collage hydrophobe et oléophobe pour matériaux cellulosiques Download PDF

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Publication number
EP0543363B1
EP0543363B1 EP92119704A EP92119704A EP0543363B1 EP 0543363 B1 EP0543363 B1 EP 0543363B1 EP 92119704 A EP92119704 A EP 92119704A EP 92119704 A EP92119704 A EP 92119704A EP 0543363 B1 EP0543363 B1 EP 0543363B1
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Prior art keywords
water
oil
paper
sizing
aldoketene
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Expired - Lifetime
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EP92119704A
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German (de)
English (en)
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EP0543363A1 (fr
Inventor
Kyle J. Bottorff
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Hercules LLC
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Hercules LLC
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
    • C07D305/02—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D305/10—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having one or more double bonds between ring members or between ring members and non-ring members
    • C07D305/12—Beta-lactones
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03—Non-macromolecular organic compounds
    • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/17—Ketenes, e.g. ketene dimers

Definitions

  • This invention relates to sizing agents for paper, and particularly to sizing agents that impart both oil and water sizing properties to paper.
  • Examples of end use products requiring some combination of water, hot-water, oil or hot-oil resistance include textile products, leather goods, reprographic paper, food board containers, wax coated paper, labels, coupons, food wrap, pet food containers, nonwoven medical wear, candy wraps, food containers for use in microwave ovens, and molded food containers.
  • any chemical additive such as a sizing agent, must be either readily water dispersible in its neat form, or easily convertible into a water dispersible emulsion or stable aqueous dispersion.
  • Sizing agents in aqueous delivery systems There are two physical forms of sizing agents in aqueous delivery systems: monomolecularly dispersed ionic salts and dispersions or emulsions of particulates or oils. Sizing agents in particulate form must be low-melting solids or liquids so the material will spread throughout the paper when heated in the dryer section of a paper machine.
  • the sizing agent When the sizing agent is added to the pulp slurry (internal addition) it must adhere to the pulp or it will not be retained in the paper. This may be accomplished by means of opposite charge attractions between the pulp and the size and by physical trapping of particles of size during web formation.
  • both hydrophobic and oleophobic constituents of the size molecules must be oriented away from the paper and hydrophilic constituents oriented towards the paper, so that liquid penetrants are exposed to a low surface energy hydrophobic and oleophobic surface.
  • the sizing agent must maintain that molecular orientation to function efficiently. This orientation can be maintained by opposite charge bonding, ionic bonding, or by covalent bonding between the size and the pulp. Covalent bonding is the strongest form of bonding. Weaker opposite charge and ionic bonds are more susceptible to cleavage by aqueous liquid penetrants, especially when the penetrants are hot.
  • Efficient commercial oil sizing agents for paper also contain hydrophilic functional groups, such as phosphate, carboxylate, or chromium salts, that maintain water dispersibility, which is needed to enable the size to be applied to the paper in an aqueous vehicle, the most practical way.
  • hydrophilic functional groups such as phosphate, carboxylate, or chromium salts
  • the most efficient oil-sizing agents for cellulosic materials contain long, linear fluorocarbon chains. Fluorocarbons, in general, have very low surface energies and are not wet easily by oil-based materials, but salts that contain fluorocarbon hydrophobes are inefficient water sizing agents. Some agents that contain fluorocarbon hydrophobes but no hydrophilic salt groups do provide both water and oil sizing, but their level of water sizing is very low. Conversely, chemicals that contain hydrocarbon hydrophobes are efficient water sizing agents, but are inefficient oil-sizing agents. Consequently, in a combination of a fluorocarbon-based product for oil resistance and a hydrocarbon-based product for water resistance, each product has an adverse effect on the other's performance.
  • a hydrocarbon-based size such as an alkyl ketene dimer (AKD) decreases the ability of a fluorochemical size to resist oil and grease penetration and requires more fluorochemical to attain the required level of oil resistance.
  • AKD alkyl ketene dimer
  • Ketene dimers which are ⁇ -lactones of 3-hydroxy-3-butenoic acids, have the generic structure When R' and R''' are hydrogen, the compounds are referred to as aldoketene dimers.
  • aldoketene dimer in which R, R', R'', and R''' are H is the one commonly referred to as ketene dimer.
  • the preparation of the aldoketenes is well known, for instance from S. Patai, "The Chemistry or Ketenes, Allenes, and Related Compounds", J.
  • R and R'' are long chain alkyl groups.
  • R groups that contain alkyl, ester, ketone, ether, isocyanate, aryl, chloro, bromo, and heptafluoroisopropoxy functionalities are included in the alkyl ketene dimer (AKD) that is sold commercially as a sizing agent for cellulosic materials.
  • R and R'' are long chain alkyl groups.
  • R groups that contain alkyl, ester, ketone, ether, isocyanate, aryl, chloro, bromo, and heptafluoroisopropoxy functionalities are examples of R and R'' include R groups that contain alkyl, ester, ketone, ether, isocyanate, aryl, chloro, bromo, and heptafluoroisopropoxy functionalities.
  • U.S. Patent 3,795,684 discloses a heptafluoroisopropoxy group on a ⁇ -lactone, but fails to suggest that its sizing ability extends beyond "water repellency" which follows from the fact that the fluorinated segment of the molecule is very short and branched.
  • A may also represent -S(CH 2 ) 1-20 H (to form a thioether), -S(CF 2 ) 1-12 F, or (to form a tertiary amine), and B may also represent -S- or Preferably, the amine is in a slight molar excess. Also preferably, the maximum alkyl chain length is 14, more preferably it is 9.
  • the carboxylic acid chlorides which are known from, for instance, U.S. Patents 3,016,406 and 3,145,222, may be made by the treatment with thionyl chloride, oxalyl chloride, phosphorous pentachloride, or phosphorous trichloride, of a fluorinated carboxylic acid having the structure: F(CF 2 ) y ZCO 2 H in which y, Z, and n are as described previously.
  • the perfluorinated ketene dimers of the invention exhibit unusually high levels of both water and oil repellency when applied to paper and shaped articles made from cellulosic materials.
  • An advantage of these compounds is that they can be emulsified in water to make sizing treatment compositions according to the invention, that impart an efficient combination of oil, hot-oil, water and hot-water sizing that impart water, hot-water, oil, and hot-oil repellency, and comprise:
  • the sizing compositions may also contain water-soluble cationic polyamine or polyamide epoxide resins to enhance emulsion stability, chemical retention, and performance. They can be added internally as the paper is being formed in a conventional manner or applied to preformed paper. Surface application of the aldoketene dimers to paper may also be made from organic solvent solutions.
  • This new class of sizing composition can be referred to as fluorinated alkyl ketene dimer dispersions/emulsions and represented for convenience by the abbreviation R f AKD.
  • the invention particularly contemplates their use to impart water, hot-water, oil, and hot-oil resistance to biodegradable cellulose molded articles, thus providing an alternative to non-biodegradable polystyrene.
  • y 4-14, and also preferably a slight molar excess of triethyl amine is present (1.02 to 1.25 molar equivalents, more preferably 1.04 to 1.12 and most preferably 1.08 molar equivalents).
  • Z has other values and substituents
  • the acid chloride is preferably added to the amine at a controlled rate such that the temperature of the reaction medium remains between zero and 90°C, more preferably between 20° and 50°C and most preferably between 40° and 45°C.
  • the desired temperature is conventionally determined according to such known factors as reagent solubility and product stability.
  • the use of a trialkyl amine other than the preferred triethyl amine is limited by conventional considerations to avoid alkyl groups that are too bulky to hinder the progress of the reaction.
  • the standard procedure includes sparging the solvent with an inert gas and maintaining an inert gas atmosphere, however, this is not a necessity of the invention.
  • the dimer product can be dissolved in ether and extracted with water and brine to remove traces of triethylammonium hydrochloride from the product.
  • the ether solution would then be dried and concentrated under reduced pressure to provide the dimer in a more pure state; however, this is not a necessity of the invention.
  • nucleophiles such as alcohols, thiols, primary amines, and secondary amines
  • Some transition metal catalysts can be used in place of the free radical catalysts, as disclosed, for instance, by C. Qing-yun and Y. Nong-yu, Acta Chim. Sinica 1118, 1985, C. Qing-yun and Z-Y. Yang J. Fluor. Chem., 28, 399, 1985, K.
  • Fluorinated carboxylic acids can also be conventionally prepared from perfluoroalkylsulfonyl chlorides. Many perfluoroalkyl halides and terminally unsaturated carboxylic acids are sold commercially.
  • the unsaturated ⁇ -lactone moiety of the fluorinated aldoketene dimer structures can be identified by the following analysis techniques:
  • the perfluorinated alkyl moiety [F(CF 2 )n-] can be identified by:
  • the aqueous R f AKD dispersions/emulsions are very stable. Outstanding oil, grease and water resistant paper can be achieved by convenient, direct addition of the R f AKD dispersions/emulsions to the pulp slurry as the paper is being made or by surface application after the paper is formed.
  • the R f AKD can also be surface applied to preformed paper from an organic solvent solution. They are not precipitated by cations from hard water, unlike the anionic salts contained in commercial oil-sizing agents, and the use of water softening agents is avoided.
  • the R f AKD sizing agents of the invention form covalent bonds to cellulose fibers under conditions existing on commercial paper machines using the heat from the paper machine, and thus avoid disruption of the bonding by acidic, basic, or neutral aqueous penetrants.
  • Emulsions/dispersions are preferably prepared by homogenization of an aqueous mixture of cooked starch, sodium lignin sulfonate (SLS), melted R f AKD, or R f AKD dissolved in a non-water miscible solvent, and sodium naphthalene sulfonate (SNS).
  • SLS sodium lignin sulfonate
  • R f AKD melted R f AKD
  • R f AKD dissolved in a non-water miscible solvent
  • SNS sodium naphthalene sulfonate
  • a bacteriostat can be added as a preservative if needed.
  • the ratios by weight on a dry basis are 0.5-6.0 parts cationic starch, preferably 0.7-3.0 parts starch, and most preferably 1.09 parts starch, 0.05-0.50 parts SLS, preferably 0.07-0.030 parts SLS, and most preferably 0.19 SLS, 0.05-0.50 parts of SNS, preferably 0.10-0.30, and most preferably 0.17 parts of sodium naphthalene sulfonate, 0.01-25 parts of R f AKD, preferably 3-20 parts of R f AKD, and most preferably 4.5-12 parts of R f AKD, and 65-99 parts of water, preferably 80-96 parts water and most preferably 85-94 parts of water.
  • the most preferred starch is a low molecular weight (7 centipoise viscosity at 5% starch in water), tertiary amine derivative (0.27% N) starch.
  • a wide variety of starches can be used. These include starches of varying molecular weight and varying degree of tertiary amine or quaternary amine derivation.
  • Surfactants other than SLS and sodium naphthalene sulfonate can also be used.
  • the R f AKD materials be in a liquid state during homogenization to make a stable, efficient sizing emulsion/dispersion. This can be accomplished by adding the R f AKD as a non-aqueous miscible solvent solution or by homogenizing the mixture at a temperature above the melting point of the R f AKD. The organic solvents can be removed from the emulsion/dispersion under reduced pressure.
  • the homogenization can be accomplished at 3000-9500 psi, more preferably at 5000-8500 psi, and most preferably at 7000-7500 psi.
  • the R f AKD emulsion/dispersions are characterized by their milky off-white to white appearance.
  • their average emulsion droplet/dispersion particle size is 0.10-1.50 microns, more preferably 0.20-0.80 microns, and most preferably 0.25-0.35 microns.
  • Such emulsion/dispersions are sufficiently stable to avoid agglomeration over a period of months at ambient temperatures.
  • Emulsion/dispersions having an average particle size greater than 0.70 are stable for short periods, but begin phase separation after standing for 30 minutes.
  • the acid chloride may need to be heated prior to addition to assure a totally liquid form of the acid chloride was being added to the reaction mixture. After addition of the acid chloride was complete, the reaction mixture was heated and held at 40-45°C for 60-90 minutes. The reaction was filtered and the filter cake (triethylammonium hydrochloride) was rinsed with anhydrous ether or 1,2-dichloropropane (DCP). The ether and DCP were warmed to 25-75°C prior to rinsing. The combined filtrates are concentrated under reduced pressure to provide fluorinated ⁇ -lactone aldoketene dimer. The dimer product is dissolved in ether and extracted with water and brine to remove traces of triethylammonium hydrochloride from the product, and the ether solution dried and concentrated under reduced pressure to provide the dimer in a more pure state.
  • Additional characteristic spectra data include: H 1 NMR (CDCl 3 ) Olefinic protons next to perfluoroalkyl come at 6.4 and 5.1 ppm as complex multiplets, all allylic protons come between 2-2.5 ppm; C 13 NMR (CDCl 3 )(proton decoupled spectra) olefinic carbons next to perfluoroalkyl come at 143.2 and 116.9 ppm.
  • the combined mixture was passed through a homogenizer at 3000-4000 psi two times to give a milky white emulsion.
  • the organic solvent was removed from the emulsion under reduced pressure. After cooling to 25°C, the average particle size of the emulsions fell between 0.20 and 0.85 microns.
  • the emulsion remains stable to agglomeration for several weeks.
  • a commercial bacteriostat, such as N-521® Biocide made by Stauffer Chemical Company (Westport, CN), is added (0.02-0.06 parts) when the emulsion is to be stored. N.B.
  • the fluorinated aldoketene dimer may be added neat to the warm starch solution followed by homogenization at 7000-8000 psi. The starch solution must be warm enough to melt the particular dimer used prior to homogenization.
  • Organic Solvent Method Samples of fluorinated aldoketene dimers were dissolved in chloroform or tetrahydrofuran (THF). Paper strips were dipped in the solvent solutions containing the test sizing agents, air dried, wetted with water on a one-nip two-roll press, and drum dried at 104°C for 20 seconds. The amount of size on the paper was calculated based on the weight of the solvent solution picked up by the paper strip. The sizes were applied to the paper at levels varying from 0.07 to 0.35 weight percent.
  • Table 3 gives the sizing results from the organic solvent method.
  • Emulsion/Dispersion Method - Paper strips were passed through a single-nip two-roll press containing dilutions of the dimer emulsions/dispersions and drum dried at 104°C for 20 seconds. The amount of size on the paper was calculated based on the weight of the aqueous emulsion/dispersion picked up by the paper strip. The sizes were applied to the paper at levels varying from 0.07 to 0.35 weight percent.
  • Table 4 gives the sizing results from the emulsion/dispersion method.
  • HAT relative degree of water resistance
  • Boiling boat test the hot-water resistance
  • oil resistance the modified kit test #
  • hot-oil resistance hot corn-oil float test
  • the change in reflectance of paper is measured as an aqueous solution of dye penetrates from the other side.
  • the liquid is contained in a ring on top of the paper, and the change in reflectance is measured photoelectrically from the bottom.
  • a convenient end point is chosen, for example, a reduction in reflected light of 20%.
  • the instrument contains a timer that stops automatically when the reflected light falls below the chosen end point.
  • An aqueous solution of naphthol green dye and 1% formic acid were used in the following experiments. As the time increases, the resistance to water penetration increases. Unsized paper will fail after zero seconds, lightly sized paper will register times ranging from 5-20 seconds, moderately sized paper from 21-100, well sized paper from 101-400 seconds, and hard sized paper from 401-2000 seconds.
  • Kit Test Solution Mixtures Kit Number Castor Oil (ml) Toluene (ml) Heptane (ml) 1 200 0 0 2 180 10 10 3 160 20 20 4 140 30 30 5 120 40 40 6 100 50 50 7 80 60 60 8 60 70 70 9 40 80 80 10 20 90 90 11 0 100 100 12 0 90 110 13 0 70 130 14 0 50 150 15 0 30 170 16 0 0 200
  • Tables 3 and 4 illustrate that the most useful commercial sizing agents do not provide as much sizing efficiency as R f AKD materials of this invention in all four sizing areas at the same time (water, hot-water, oil, and hot-oil sizing).
  • R f AKD emulsion/dispersions were added to the pulp fiber during production of molded fiber articles.
  • Recycled newspapers were used as fiber furnish and the articles were molded at a pH of 7.5.
  • the articles were formed on a pilot scale (Table 5) molded fiber paper machine and dried in a convection oven at 135-162°C to a moisture content of 0-18% by weight, preferably 2-8% by weight.
  • Hot Water Test Distilled water at 95-100°C is poured onto a molded fiber article. After 15 minutes the water was poured off and the article was examined for surface wetting and penetration by the water. The less surface wetting and penetration the better the water sizing.
  • Hot Oil Test Corn oil at 83-95°C was poured onto a molded fiber article. After 15 minutes the article was examined for surface wetting and penetration by the oil. The less surface wetting and penetration the better the oil sizing.
  • Oil Pickup Equal portions of 83-95°C corn oil were poured onto preweighed molded fiber articles of equal moisture content and allowed to stand for 15 minutes. The oil was gravity drained from the articles for 45 minutes and any excess oil remaining on the articles is removed with a clean cloth or towel. The weight of the oil picked up by the article was then determined. The lower the weight of oil pickup the better the oil sizing.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Epoxy Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Claims (6)

  1. Aldocétène dimérique répondant à la structure suivante :
    Figure 00430001
    où y = 1-18,
       Z = (CH2)n,
    Figure 00430002
    ou CH=CH(CH2)n-2, et n est un nombre entier de 3-18 inclusivement, ou
    Figure 00430003
    où n est un nombre entier de 3-18 inclusivement, et
       A = -O(CH2)1-20H,
    Figure 00430004
    Figure 00430005
    -C(CF2)1-12F, ou -H, et B = -O-,
    Figure 00430006
    ou
    Figure 00440001
  2. Aldocétène dimérique suivant la revendication 1, caractérisé en ce qu'il répond à la structure :
    Figure 00440002
    où y = 1-18,
    Z = (CH2)n,
    Figure 00440003
    ou CH=CH(CH2)n-2 et n est un nombre entier de 3-18 inclusivement.
  3. Procédé de préparation d'un aldocétène dimérique suivant l'une quelconque des revendications 1 ou 2, comprenant le mélange à une trialkylamine et dans un solvant organique aprotiqùe d'un chlorure d'acide carboxylique fluoré, ou d'un mélange de tels chlorures, caractérisé en ce que le chlorure d'acide carboxylique fluoré répond à la structure suivante :
    Figure 00440004
    où y = 1,18,
    Z = (CH2)n,
    Figure 00450001
    ou CH=CH(CH2)n-2 et n est un nombre entier de 3-18, ou
    Figure 00450002
    ou
    A = -O(CH2)1-20H,
    Figure 00450003
    Figure 00450004
    -C(CF2)1-12F, ou -H, et B = -O-,
    Figure 00450005
  4. Procédé de préparation d'un aldocétène dimérique suivant la revendication 3, caractérisé en ce que le chlorure d'acide carboxylique fluoré répond à la structure suivante :
    Figure 00450006
    où y = 1-18,
    Z = (CH2)n,
    Figure 00460001
    ou CH=CH(CH2)n-2 et n est un nombre entier de 3-18.
  5. Procédé suivant la revendication 3 ou 4, caractérisé en ce que l'amine est présente en un léger excès molaire par rapport au chlorure d'acide carboxylique fluoré et on entreprend la réaction dans un solvant aprotique.
  6. Utilisation d'un aldocétène dimérique suivant la revendication 1 ou 2, dans une composition de collage qui confère une répulsion vis-à-vis de l'eau , de l'eau chaude, de l'huile et de l'huile chaude et qui comprend ledit aldocétène dimérique, de l'amidon cationique, un émulsif et de l'eau.
EP92119704A 1991-11-18 1992-11-19 Dimères fluorés d'aldocetènes, et leur utilisation comme agents de collage hydrophobe et oléophobe pour matériaux cellulosiques Expired - Lifetime EP0543363B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US794087 1991-11-18
US07/794,087 US5252754A (en) 1991-11-18 1991-11-18 Fluorinated aldoketene dimer structures and their use as combination oil and water resistant sizes for cellulosic materials

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EP0543363A1 EP0543363A1 (fr) 1993-05-26
EP0543363B1 true EP0543363B1 (fr) 1998-01-21

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US (1) US5252754A (fr)
EP (1) EP0543363B1 (fr)
JP (1) JPH0625204A (fr)
DE (1) DE69224155T2 (fr)
FI (1) FI104820B (fr)
MX (1) MX9206641A (fr)

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GB9309604D0 (en) * 1993-05-10 1993-06-23 Hercules Inc Process for the manufacture of alkyl ketene dimer
CA2146726A1 (fr) 1994-05-18 1995-11-19 Susan S. Harrison Phosphates renfermant du fluor
US6027611A (en) * 1996-04-26 2000-02-22 Kimberly-Clark Worldwide, Inc. Facial tissue with reduced moisture penetration
US6175022B1 (en) * 1998-12-30 2001-01-16 Hercules Incorporated Alcohol-terminated ketene multimer sizing agents
US20050252628A1 (en) * 2004-05-11 2005-11-17 Day James F Stabilizing compositions
US7799169B2 (en) 2004-09-01 2010-09-21 Georgia-Pacific Consumer Products Lp Multi-ply paper product with moisture strike through resistance and method of making the same
US7271308B2 (en) * 2004-10-19 2007-09-18 Hercules Incorporated Process for isomerization of alpha olefins to internal olefins
US20070261807A1 (en) * 2006-05-12 2007-11-15 Taggart Thomas E Use of polyvinylamine to improve oil and water sizing in cellulosic products
CA2667752C (fr) 2006-10-27 2013-08-06 Crane & Co., Inc. Document de securite resistant a la terre et/ou a l'humidite
US20080163993A1 (en) * 2007-01-10 2008-07-10 Varnell Daniel F Surface sizing with sizing agents and glycol ethers
FR2928383B1 (fr) 2008-03-06 2010-12-31 Georgia Pacific France Feuille gaufree comportant un pli en materiau hydrosoluble et procede de realisation d'une telle feuille.
WO2010033536A2 (fr) 2008-09-16 2010-03-25 Dixie Consumer Products Llc Feuille de base d'emballage alimentaire a microfibre de cellulose regeneree
US8663427B2 (en) 2011-04-07 2014-03-04 International Paper Company Addition of endothermic fire retardants to provide near neutral pH pulp fiber webs
WO2012018749A1 (fr) 2010-08-03 2012-02-09 International Paper Company Bande de pâte défibrée ignifugée et son processus de fabrication
US20120107511A1 (en) 2010-11-01 2012-05-03 Georgia-Pacific Consumer Products Lp Method Of Applying Fugitive Hydrophobic Treatment To Tissue Product
US8388807B2 (en) 2011-02-08 2013-03-05 International Paper Company Partially fire resistant insulation material comprising unrefined virgin pulp fibers and wood ash fire retardant component

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US3362965A (en) * 1965-12-08 1968-01-09 Du Pont Beta-lactones of 3-hydroxy-4, 4-bis(perfluoroalkyl)-3-butenoic acids and their method of preparation
US3795684A (en) * 1972-10-27 1974-03-05 Nalco Chemical Co Ketene dimers from long chain alkanoic acids with perfluoroalkyl terminal segments
US4419298A (en) * 1981-08-12 1983-12-06 Ciba-Geigy Corporation Ethanolamine salts of di-perfluoroalkyl group containing acids
US4426466A (en) * 1982-06-09 1984-01-17 Minnesota Mining And Manufacturing Company Paper treatment compositions containing fluorochemical carboxylic acid and epoxidic cationic resin
DE3407361A1 (de) * 1984-02-29 1985-08-29 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von hydrophobier- und oleophobiermittel

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DE69224155T2 (de) 1998-05-07
FI925246A (fi) 1993-05-19
DE69224155D1 (de) 1998-02-26
FI104820B (fi) 2000-04-14
FI925246A0 (fi) 1992-11-18
MX9206641A (es) 1993-05-01
US5252754A (en) 1993-10-12
EP0543363A1 (fr) 1993-05-26
JPH0625204A (ja) 1994-02-01

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